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. Author manuscript; available in PMC: 2018 Mar 1.
Published in final edited form as: Obstet Gynecol. 2017 Mar;129(3):465–472. doi: 10.1097/AOG.0000000000001889

Table 3.

Association of abnormal maternal serum analytes in relation to placental abruption with and without co-occurring ischemic placental disease

No IPD
Placental abruption only
Abruption with preeclampsia or FGR
No. (%) No. (%) Risk ratio (95% CI)
No. (%) Risk ratio (95% CI)
Unadjusted Adjusted Unadjusted Adjusted
PAPP-A ≤5 percentile 1,745 (6.1) 20 (10.6) 1.8 (1.2–2.9) 1.8 (1.2–2.9) 4 (16.7) 3.1 (1.1–9.0) 2.8 (1.0–8.3)
Maternal serum AFP ≥95 percentile 1,556 (5.8) 20 (10.4) 1.9 (1.2–3.0) 1.8 (1.1–3.1) 3 (15.0) 2.9 (0.8–9.8) 2.7 (0.8–9.2)
Inhibin-A ≤5 percentile 1,630 (6.0) 18 (10.2) 1.8 (1.1–2.9) 1.8 (1.1–2.9) 1 (7.1) 0.5 (0.2–9.2) 1.3 (0.2–9.8)
Inhibin-A ≥95percentile 1,484 (5.5) 15 (8.7) 1.6 (1.0–2.8) 1.6 (0.9–2.7) 8 (38.1) 10.5 (4.4–25.3) 8.3 (3.4–21.1)

IPD, ischemic placental disease; FGR, fetal growth restriction; PAPP-A, pregnancy-associated plasma protein A; AFP, alpha fetoprotein; CI, confidence interval

Risk ratios are adjusted for maternal age, age-squared, primiparity, maternal education, single marital status, race-ethnicity, and smoking, with “no ischemic placental disease” as the reference group